2023 - Research.com Chemistry in United States Leader Award
2020 - Member of the National Academy of Sciences
2018 - Fellow of the American Academy of Arts and Sciences
F. Dean Toste mainly focuses on Catalysis, Organic chemistry, Enantioselective synthesis, Medicinal chemistry and Intramolecular force. His work deals with themes such as Combinatorial chemistry, Reactivity and Molecule, which intersect with Catalysis. Organic chemistry is closely attributed to Biomass in his research.
His Enantioselective synthesis study combines topics from a wide range of disciplines, such as Yield, Computational chemistry, Stereochemistry and Cyclopropanation. His biological study spans a wide range of topics, including Cationic polymerization, Aryl and Photochemistry. His study in Intramolecular force is interdisciplinary in nature, drawing from both Cyclopentanes, Alkene and Ene reaction.
The scientist’s investigation covers issues in Catalysis, Organic chemistry, Enantioselective synthesis, Combinatorial chemistry and Medicinal chemistry. His biological study focuses on Nucleophile. In his work, Fermentation is strongly intertwined with Biomass, which is a subfield of Organic chemistry.
His work investigates the relationship between Enantioselective synthesis and topics such as Phase that intersect with problems in Ion. F. Dean Toste combines subjects such as Supramolecular chemistry, Allylic rearrangement and Substrate with his study of Combinatorial chemistry. His work in Medicinal chemistry covers topics such as Propargyl which are related to areas like Annulation.
His primary areas of study are Catalysis, Combinatorial chemistry, Enantioselective synthesis, Selectivity and Reactivity. Catalysis is a primary field of his research addressed under Organic chemistry. His Combinatorial chemistry research incorporates elements of Reagent and Oxaziridine, Stereochemistry.
Within one scientific family, F. Dean Toste focuses on topics pertaining to Phosphoric acid under Enantioselective synthesis, and may sometimes address concerns connected to Allylic rearrangement. The various areas that he examines in his Selectivity study include Yield, Substituent, Toluene, Cationic polymerization and Double bond. The Reactivity study combines topics in areas such as Nanoparticle, Monolayer, Carbene, Redox and Methionine.
F. Dean Toste mainly investigates Catalysis, Combinatorial chemistry, Enantioselective synthesis, Organic chemistry and Nanotechnology. His Catalysis research integrates issues from Chemical substance, Molecular recognition and Dendrimer. F. Dean Toste interconnects Enantiomeric excess, Aldol reaction, Stereocenter, Stereochemistry and Carbon chemistry in the investigation of issues within Combinatorial chemistry.
The study incorporates disciplines such as Reagent, Computational chemistry, Cyclopentene and Medicinal chemistry in addition to Enantioselective synthesis. His Organic chemistry study integrates concerns from other disciplines, such as Biomass and Chemical synthesis. His biological study deals with issues like Molecule, which deal with fields such as Affinities.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Ligand effects in homogeneous Au catalysis.
David J. Gorin;Benjamin D. Sherry;F. Dean Toste.
Chemical Reviews (2008)
Relativistic effects in homogeneous gold catalysis
David J. Gorin;F. Dean Toste.
Nature (2007)
Advances in catalytic enantioselective fluorination, mono-, di-, and trifluoromethylation, and trifluoromethylthiolation reactions.
Xiaoyu Yang;Tao Wu;Robert J. Phipps;F. Dean Toste.
Chemical Reviews (2015)
A powerful chiral counterion strategy for asymmetric transition metal catalysis.
Gregory L. Hamilton;Eun Joo Kang;Miriam;F. Dean Toste.
Science (2007)
Supramolecular Catalysis in Metal–Ligand Cluster Hosts
Casey J. Brown;F. Dean Toste;Robert G. Bergman;Robert G. Bergman;Kenneth N. Raymond;Kenneth N. Raymond.
Chemical Reviews (2015)
The progression of chiral anions from concepts to applications in asymmetric catalysis
Robert J. Phipps;Gregory L. Hamilton;F. Dean Toste.
Nature Chemistry (2012)
Gold(I)-catalyzed stereoselective olefin cyclopropanation.
Magnus J. Johansson;David J. Gorin;Steven T. Staben;F. Dean Toste.
Journal of the American Chemical Society (2005)
Gold(I)-Catalyzed Intramolecular Acetylenic Schmidt Reaction
David J. Gorin;Nicole R. Davis;F. Dean Toste.
Journal of the American Chemical Society (2005)
Asymmetric electrophilic fluorination using an anionic chiral phase-transfer catalyst
Vivek Rauniyar;Aaron D. Lackner;Gregory L. Hamilton;F. Dean Toste.
Science (2012)
Gold(I)-Catalyzed Conia-Ene Reaction of β-Ketoesters with Alkynes
Joshua J. Kennedy-Smith;Steven T. Staben;F. Dean Toste.
Journal of the American Chemical Society (2004)
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